The 21st Annual Meeting of the Protein Science Society of Japan

Presentation information

Poster Session

[3P-1] Poster 3 (3P-01ー3P-47)

Fri. Jun 18, 2021 3:15 PM - 5:15 PM Poster 1

[3P-28] Recognition mechanism of a monoclonal antibody which neutralizes different species of flavivirus

Jun Kobayashi1, Tatsuhiko Ozawa2, Hideyuki Masaki3, Ryuichi Kato1 (1.SBRC, IMSS, High Energy Accelerator Research Organization (KEK), 2.Dept. Immunol., Fac. Med., Univ. of Toyama, 3.Faculty of Biology-Oriented Science and Technology, Kindai Univ.)

West Nile Virus (WNV), which is one of the flavivirus family, causes West Nile fever and lethal encephalitis and is distributed throughout the world. We established a monoclonal antibody (WN_83) from Japanese Encephalitis Virus (JEV) - vaccinated volunteers. WN_83 neutralizes not only JEV but also WNV. To elucidate the mechanism how WN_83 recognizes both viruses, we determined a crystal structure of the antigen-antibody complex.
The Fab fragment of WN_83 and the domain III of the WNV envelope protein (WNVE DIII) complex was isolated by SEC. We obtained the 2.5 Å resolution structure from cluster crystals by using the automated crystallization robot, PXS2 in KEK and the automated data collection system, ZOO in SPring-8.
Both CDR3s interacted with Arg388 of WNVE DIII. Site-directed mutagenesis and ELISA showed that Arg388 is critical for the binding. Sequence alignment showed that Arg388 is conserved in the envelope protein of JEV (JEVE). In addition, several residues of the CDR-L1 and L3 interacted with WNVE DIII. The residues were not identical but similar in JEVE. These results suggest that the cross-reaction is probably caused by (1) the recognition of Arg388 conserved in JEVE and WNVE, and (2) the tolerance of the CDRs in the L chain.